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Omegaven Expanded Access Protocol

Protocol for Patients With Parenteral Nutrition Associated Liver Disease (PNALD) to Access Parenteral Fish Oil (Omegaven®) - Omegaven IND 122375

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT02121769
Enrollment
Unknown
Registered
2014-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2019-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parenteral Nutrition Associated Liver Disease

Keywords

cholestasis, short bowel syndrome

Brief summary

Omegaven is an intravenous fat emulsion (IFE) comprised of omega-3 fatty acids derived from fish oil. It will be used in an open label compassionate use treatment protocol, as an alternative to soybean oil (omega-6), as the sole IFE source of parenteral nutrition in an effort to reduce and/or reverse parenteral nutrition associated liver disease. The study will evaluate the safety and efficacy of Omegaven use in pediatric patients with PN dependence and PNALD.

Interventions

DRUGOmegaven

10% Omegaven 1g/kg/day, Intravenous by continuous infusion in conjunction with parenteral nutrition, until the patient no longer requires parenteral nutrition or until participation in the study is terminated.

Sponsors

St. Luke's Health System, Boise, Idaho
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
No minimum to 17 Years

Inclusion criteria

* Patients will be PN dependent (unable to meet nutritional needs solely by enteral nutrition) and are expected to require PN for at least another 30 days * Parenteral nutrition associated liver disease (PNALD) as defined as a direct bilirubin of ≥ 2 mg/dL on the last two consecutive bilirubins while on PN. Other causes of liver disease should be excluded. A liver biopsy is not necessary for treatment. * Failed standard/conventional therapies to prevent progression of PNALD. * Age newborn to 17 years of age * Signed informed consent.

Exclusion criteria

* Allergy to eggs and/or shellfish * Female who is pregnant or lactating * Severe hemorrhagic disorder * Other causes of chronic liver disease (Hepatitis C, Cystic fibrosis, biliary atresia, and alpha 1 anti-trypsin deficiency,) * 18 years of age or older * Parent/legally authorized representative is unwilling to consent.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026